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This classifies it into root causes — undeclared allergen, sterility failure, nitrosamine impurity, software defect, component recall — and scores firms that keep failing the same way. 89.4% classified over 900 live recalls.", "version": "0.1", "x-build-id": "Qy9qSU8y1K6Sievnh" }, "servers": [ { "url": "https://api.apify.com/v2" } ], "paths": { "/acts/datalayer~fda-recall-enforcement/run-sync-get-dataset-items": { "post": { "operationId": "run-sync-get-dataset-items-datalayer-fda-recall-enforcement", "x-openai-isConsequential": false, "summary": "Executes an Actor, waits for its completion, and returns Actor's dataset items in response.", "tags": [ "Run Actor" ], "requestBody": { "required": true, "content": { "application/json": { "schema": { "$ref": "#/components/schemas/inputSchema" } } } }, "parameters": [ { "name": "token", "in": "query", "required": true, "schema": { "type": "string" }, "description": "Enter your Apify token here" } ], "responses": { "200": { "description": "OK" } } } }, "/acts/datalayer~fda-recall-enforcement/runs": { "post": { "operationId": "runs-sync-datalayer-fda-recall-enforcement", "x-openai-isConsequential": false, "summary": "Executes an Actor and returns information about the initiated run in response.", "tags": [ "Run Actor" ], "requestBody": { "required": true, "content": { "application/json": { "schema": { "$ref": "#/components/schemas/inputSchema" } } } }, "parameters": [ { "name": "token", "in": "query", "required": true, "schema": { "type": "string" }, "description": "Enter your Apify token here" } ], "responses": { "200": { "description": "OK", "content": { "application/json": { "schema": { "$ref": "#/components/schemas/runsResponseSchema" } } } } } } }, "/acts/datalayer~fda-recall-enforcement/run-sync": { "post": { "operationId": "run-sync-datalayer-fda-recall-enforcement", "x-openai-isConsequential": false, "summary": "Executes an Actor, waits for completion, and returns the OUTPUT from Key-value store in response.", "tags": [ "Run Actor" ], "requestBody": { "required": true, "content": { "application/json": { "schema": { "$ref": "#/components/schemas/inputSchema" } } } }, "parameters": [ { "name": "token", "in": "query", "required": true, "schema": { "type": "string" }, "description": "Enter your Apify token here" } ], "responses": { "200": { "description": "OK" } } } } }, "components": { "schemas": { "inputSchema": { "type": "object", "properties": { "productTypes": { "title": "Product types", "type": "array", "description": "Which FDA enforcement endpoints to read. Each is independent — a gap in one does not affect the others.", "items": { "type": "string", "enum": [ "drug", "device", "food" ], "enumTitles": [ "Drugs", "Medical devices", "Food" ] }, "default": [ "drug", "device", "food" ] }, "searchTerm": { "title": "Search term", "type": "string", "description": "Matched against the recall reason and the product description, e.g. insulin, catheter, peanut.", "default": "" }, "firm": { "title": "Recalling firm", "type": "string", "description": "Restrict to one company, e.g. Abbott. Matched against the recalling firm name.", "default": "" }, "classifications": { "title": "Recall classification", "type": "array", "description": "Class I means a reasonable probability of serious injury or death. 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